A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437872



Internal ID22104053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39291894..39292501hg38UCSC Ensembl
chr17:37448147..37448754hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758658
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437872
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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